Studying Long QT Syndrome Caused by NAA10 Genetic Variants Using Patient-Derived Induced Pluripotent Stem Cells

Author:

Belbachir Nadjet12,Wu Yiyang34,Shen Mengcheng12ORCID,Zhang Sophia L.12,Zhang Joe Z.12,Liu Chun125ORCID,Knollmann Bjorn C.6ORCID,Lyon Gholson J.378,Ma Ning12910ORCID,Wu Joseph C.12115ORCID

Affiliation:

1. Stanford Cardiovascular Institute, Stanford, CA (N.B., M.S., S.L.Z., J.Z.Z., C.L., N.M., J.C.W.).

2. Division of Cardiology, Department of Medicine (N.B., M.S., S.L.Z., J.Z.Z., C.L., N.M., J.C.W.), Stanford University School of Medicine, CA.

3. Stanley Institute for Cognitive Genomics, Cold Spring Harbor Laboratory, Woodbury, NY (Y.W., G.J.L.).

4. Vanderbilt Memory & Alzheimer’s Center, Vanderbilt University Medical Center, Nashville, TN (Y.W.).

5. Greenstone Biosciences, Palo Alto, CA (C.L., J.C.W.).

6. Vanderbilt Center for Arrhythmia Research and Therapeutics, Division of Clinical Pharmacology, Vanderbilt University School of Medicine, Nashville, TN (B.C.K.).

7. Department of Human Genetics, New York State Institute for Basic Research in Developmental Disabilities, Staten Island (G.J.L.).

8. Biology PhD Program, Graduate Center, City University of New York (G.J.L.).

9. School of Basic Medical Sciences, Guangzhou Laboratory, Guangzhou Medical University, China (N.M.).

10. The Sixth Affiliated Hospital of Guangzhou Medical University, Qingyuan People’s Hospital, China (N.M.).

11. Department of Radiology (J.C.W.), Stanford University School of Medicine, CA.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Reference4 articles.

1. NAA10-related syndrome

2. Wu, Y. Toward Precision Medicine: From Clinical Genomics to iPSC Disease Modeling (Publication No. 10281516) [Doctoral dissertation, Stony Brook University]. ProQuest Dissertations Publishing; 2017. http://hdl.handle.net/11401/77611

3. NAA10 mutation causing a novel intellectual disability syndrome with Long QT due to N-terminal acetyltransferase impairment

4. Using VAAST to Identify an X-Linked Disorder Resulting in Lethality in Male Infants Due to N-Terminal Acetyltransferase Deficiency

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